Exciting pharma jobs opportunity for experienced Clinical Research Associates! Fortrea is hiring a Medical Device & Diagnostics CRA 2 for a US Remote position. Ideal for professionals seeking pharmaceutical careers in India and global exposure in medical device clinical trials.
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About the Company
Fortrea is a leading global Contract Research Organization (CRO) with decades of clinical development expertise. The company provides comprehensive clinical development and technology solutions to pharmaceutical, biotechnology, and medical device clients across more than 20 therapeutic areas.
Operating in approximately 100 countries, Fortrea is recognized for scientific rigor, innovation, regulatory compliance, and commitment to accelerating drug and device development. Its strong global presence and patient-focused approach make it a preferred partner for transforming clinical research.
Job Details
- Company Name: Fortrea
- Experience: 1-3 years of Clinical Monitoring experience
- Qualification: University or college degree or certification in a related allied health profession (e.g., nursing licensure)
- Location: United States (Remote)
- Work Type: Remote
Job Description
Fortrea is seeking an experienced Medical Device & Diagnostics CRA 2 who is French-speaking and has sponsorship to travel into Canada. This role is part of the Medical Device & Diagnostics team and involves leading site monitoring activities with 60-70% travel (7-9 days on site per month). The position offers the opportunity to work on cutting-edge medical device clinical trials in a fast-paced, technology-driven environment.
Position Title: Medical Device & Diagnostics – CRA 2
- Department: Clinical – Medical Device & Diagnostics
- Market: Contract Research Organization (CRO)
- Role: Clinical Research Associate focused on site monitoring and management
- Experience: 1-3 years
- Education/Qualification: University degree or allied health certification (e.g., Nursing)
Skills/Qualifications
- 1-3 years of Clinical Monitoring experience in medical devices
- French language proficiency (spoken and written)
- Strong clinical judgment and understanding of GCP/regulatory requirements
- Excellent communication, teamwork, and interpersonal skills
- Ability to adapt quickly to changing priorities in a fast-paced environment
- Proficiency with clinical trial technology and electronic data systems
- Willingness to travel extensively (60-70%)
- Problem-solving skills and attention to detail
Key Responsibilities
- Conduct site monitoring and close-out visits
- Ensure protocol and GCP compliance at clinical sites
- Verify informed consent and patient protection
- Review CRFs and source documents for data integrity
- Manage Serious Adverse Event reporting
- Perform query generation and resolution
- Support study feasibility and site management
- Train new employees through co-monitoring
- Coordinate designated clinical projects
- Liaise with vendors and site staff effectively
Benefits/Perks
- Competitive salary (Target Pay Range: $105,000 – $117,000)
- Comprehensive medical, dental, vision, and life insurance
- 401(K) retirement plan
- Paid Time Off (PTO) with flexible plan
- Employee recognition awards and ERGs
- Career development and learning opportunities
- Global exposure in medical device trials
How to Apply
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Fortrea career page.
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Interested candidates can apply directly through the Fortrea careers portal at www.fortrea.com. Applications are accepted on an ongoing basis.
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Apply now to advance your career in clinical research with a global CRO leader.
Why You Should Join
Fortrea offers a dynamic, collaborative culture where innovation and integrity drive success. Employees enjoy long-term career stability, continuous learning, and the chance to work on impactful medical device projects that improve patient lives worldwide. With a strong focus on regulatory compliance and professional growth, Fortrea provides an excellent environment for motivated professionals seeking meaningful pharmaceutical careers.
FAQs
Q1. What experience is required for the Medical Device CRA 2 position?
A: Candidates need 1-3 years of Clinical Monitoring experience, preferably in medical devices.
Q2. Is this a fully remote job?
A: Yes, it is a US Remote position with 60-70% travel, including to Canada.
Q3. What language skill is mandatory?
A: French speaking ability is required for this role.
Q4. How can I apply for this pharma job?
A: Submit your application online via the Fortrea careers website (www.fortrea.com).
